Results 151 to 160 of about 1,211 (180)
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Congenital insensitivity to pain with anhidrosis: case report.

Pediatric dentistry, 1990
Congenital insensitivity to pain with anhidrosis is a rare disorder. A case of a male patient presenting with loss of pain and temperature sensation, lack of sweat, and mild mental retardation is described. Differential diagnosis with similar pathological conditions is presented.
N, Kouvelas, C, Terzoglou
openaire   +1 more source

Congenital insensitivity to pain with anhidrosis

Annals of Neurology, 2015
Thomas D, Bird, Phillip D, Swanson
openaire   +2 more sources

[Congenital insensitivity to pain with anhidrosis associated with congenital myasthenic syndrome].

Revista de neurologia, 2006
Congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropathy type IV (HSAN IV) is a rare autosomal recessive disorder featuring recurrent fever episodes, inability to sweat, absent response to noxious stimuli, self mutilating behavior and mental retardation.
M, Raspall-Chaure   +7 more
openaire   +1 more source

Congenital insensitivity to pain with anhidrosis: a case report.

Electromyography and clinical neurophysiology, 2003
Congenital insensitivity to pain with anhidrosis is an extremely rare autosomal recessive disorder characterized by inexplicable episodes of hyperpyrexia, anhidrosis, insensitivity to pain and self-mutilation. Described is a 6-year-old girl with symptoms signs and electrodiagnostic finding compatible with this disease.
M R, Emad, G R, Raissi
openaire   +1 more source

Anesthesia for congenital insensitivity to pain with anhidrosis

Pediatric Anesthesia, 2007
Ozgur Canbay   +4 more
openaire   +1 more source

Congenital insensitivity to pain with anhidrosis in a child

Russian Journal of Pain, 2020
E. V. Levitina   +3 more
openaire   +1 more source

Congenital Insensitivity to Pain: A Misnomer

Journal of Pain, 2019
Asaf Weisman   +2 more
exaly  

A Novel NTRK1 Mutation Associated with Congenital Insensitivity to Pain with Anhidrosis

American Journal of Human Genetics, 1999
Angela Greco   +2 more
exaly  

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